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Spatially Resolved Molecular Dysfunction in the Prefrontal Cortex of Patients with Amyotrophic Lateral Sclerosis (ALS).
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Spatially Resolved Molecular Dysfunction in the Prefrontal Cortex of Patients with Amyotrophic Lateral Sclerosis (ALS)./
作者:
Petrescu, Joana.
面頁冊數:
1 online resource (153 pages)
附註:
Source: Dissertations Abstracts International, Volume: 84-07, Section: B.
Contained By:
Dissertations Abstracts International84-07B.
標題:
Neurosciences. -
電子資源:
http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=30244458click for full text (PQDT)
ISBN:
9798368439181
Spatially Resolved Molecular Dysfunction in the Prefrontal Cortex of Patients with Amyotrophic Lateral Sclerosis (ALS).
Petrescu, Joana.
Spatially Resolved Molecular Dysfunction in the Prefrontal Cortex of Patients with Amyotrophic Lateral Sclerosis (ALS).
- 1 online resource (153 pages)
Source: Dissertations Abstracts International, Volume: 84-07, Section: B.
Thesis (Ph.D.)--Columbia University, 2023.
Includes bibliographical references
Amyotrophic lateral sclerosis and frontotemporal dementia (ALS-FTD) represents a spectrum of neurodegenerative disease with clinical presentations ranging from progressive paralysis to cognitive impairment. Approximately 15% of ALS-FTD patients initially presenting with motor symptoms also receive a diagnosis of dementia, but a majority of these patients demonstrate some level of cognitive impairment over the course of disease. Identifying molecular pathways that contribute to the development of cognitive deficits in ALS-FTD has thus far been limited by the quality of clinical information and postmortem tissue preservation as well as available technologies. This thesis aims to investigate early stages of cognitive involvement in ALS-FTD using postmortem tissues from a cohort of non-demented ALS patients who have had cognitive and pathological phenotyping. Spatially resolved transcriptome profiling of prefrontal cortex tissues from this cohort identifies dysregulated pathways in non-motor regions, contributing to our understanding of molecular perturbations underlying cognitive impairment in ALS-FTD.
Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2023
Mode of access: World Wide Web
ISBN: 9798368439181Subjects--Topical Terms:
588700
Neurosciences.
Subjects--Index Terms:
Frontotemporal dementiaIndex Terms--Genre/Form:
542853
Electronic books.
Spatially Resolved Molecular Dysfunction in the Prefrontal Cortex of Patients with Amyotrophic Lateral Sclerosis (ALS).
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Source: Dissertations Abstracts International, Volume: 84-07, Section: B.
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Amyotrophic lateral sclerosis and frontotemporal dementia (ALS-FTD) represents a spectrum of neurodegenerative disease with clinical presentations ranging from progressive paralysis to cognitive impairment. Approximately 15% of ALS-FTD patients initially presenting with motor symptoms also receive a diagnosis of dementia, but a majority of these patients demonstrate some level of cognitive impairment over the course of disease. Identifying molecular pathways that contribute to the development of cognitive deficits in ALS-FTD has thus far been limited by the quality of clinical information and postmortem tissue preservation as well as available technologies. This thesis aims to investigate early stages of cognitive involvement in ALS-FTD using postmortem tissues from a cohort of non-demented ALS patients who have had cognitive and pathological phenotyping. Spatially resolved transcriptome profiling of prefrontal cortex tissues from this cohort identifies dysregulated pathways in non-motor regions, contributing to our understanding of molecular perturbations underlying cognitive impairment in ALS-FTD.
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